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/ Cytocolor, Inc.
Cytocolor, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K860319
MEGACOLOR
February 20, 1986
K860317
NEUTROCOLOR
February 20, 1986
K860321
LYSOCOLOR
February 20, 1986
K860320
GRANULOCOLOR
February 20, 1986
K860316
PANOPTIKON
February 20, 1986